Dr. Andreas Eitzinger
Dr. Andreas Eitzinger
M. Sc. (Dipl.-Ing.)
AK PD Dr. Ofial
Dept. Chemie
Ludwig-Maximilians-Universität München
Butenandtstr. 5-13 (Haus F)
81377 München
Germany(10/1021 - 09/2023)
Awards/Fellowships
FWF Erwin-Schrödinger-Fellowship (J-4592)
Project title: Electrophilic Reactivities of Substituted Cyclopropanes
Publications
Defining the Synthetic Scope of ortho-Quinone Methides by Quantifying Their Electrophilicity
C. Gross, A. Eitzinger, N. Hampel, P. Mayer, A. R. Ofial, Chem. Eur. J., EarlyView (DOI: 10.1002/chem.202403785).
[download] [FAIR kinetics data]
2-Methylene-1,2-dihydropyridines (2-pyNHOs): Highly Nucleophilic Enamines
A. Behnke, A. Eitzinger, Y. He, P. W. Antoni, A. R. Ofial, M. M. Hansmann, Eur. J. Org. Chem. 2024, 27, e202400373.
[download]
Pyridinium-Derived Mesoionic N-Heterocyclic Olefins (py-mNHOs)
Q. Sun, A. Eitzinger, R. Esken, P. W. Antoni, R. J. Mayer, A. R. Ofial, M. M. Hansmann, Angew. Chem. Int. Ed. 2024, 63, e202318283.
[download]
Unveiling the impact of a CF2 motif in the isothiourea catalyst skeleton: Evaluating C(3)-F2-HBTM and its catalytic activity
M. T. Westwood, K. Kasten, L. Stockhammer, R. del Río-Rodríguez, J. A. Fernández-Salas, A. Eitzinger, A. M. Z. Slawin, M. Waser, J. Alémán, A. R. Ofial, A. D. Smith, ARKIVOC 2024 (4) 202312093.
[download]
Nucleophilicity of 4-(Alkylthio)-3-imidazoline Derived Enamines
M. J. Hensinger, A. Eitzinger, O. Trapp, A. R. Ofial, Chem. Eur. J. 2024, 30, e202302764.
[download]
Pushing the Upper Limit of Nucleophilicity Scales by Mesoionic N-Heterocyclic Olefins
A. Eitzinger, J. Reitz, P. W. Antoni, H. Mayr, A. R. Ofial, M. M. Hansmann, Angew. Chem. Int. Ed. 2023, 62, e202309790.
[download]
Reactivity of electrophilic cyclopropanes
A. Eitzinger, A. R. Ofial, Pure Appl. Chem. 2023, 95, 389-400.
[download]
Access to β-Alkylated γ-Functionalized Ketones via Conjugate Additions to Arylidieneisoxazol-5-ones and Mo(CO)6-Mediated Reductive Cascade Reactions
A. Macchia, F. F. Summa, G. Monaco, A. Eitzinger, A. R. Ofial, A. Di Mola, A. Massa, ACS Omega 2022, 7, 8808-8818.
[download]